Photoinduced Diazo Carbene-Promoted C(sp<sup>3</sup>)–H Oxidative Cross-Coupling Reaction for α-Triazolation of Isochromans

A photocatalytic diazo triplet carbene-promoted C(sp<sup>3</sup>)-H oxidative coupling of isochromans and triazoles was developed in up to 83% yield at room temperature in air. The radical-like triplet carbenes were used as efficient HAT acceptors, and the possible synergistic HAT enabled the unprecedented process with a high regioselectivity.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-03-17
DOI
https://doi.org/10.1021/acs.joc.4c02722
Citations
3
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
2.81

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article

Photoinduced Diazo Carbene-Promoted C(sp3)–H Oxidative Cross-Coupling Reaction for α-Triazolation of Isochromans

Shunying Liu, Xiao Tang, Xiang Wu, Jinhua Liu
3 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
2.81
article

Photoinduced Diazo Carbene-Promoted C(sp3)–H Oxidative Cross-Coupling Reaction for α-Triazolation of Isochromans

Shunying Liu, Xiao Tang, Xiang Wu, Jinhua Liu
article en
3 citations

Abstract

A photocatalytic diazo triplet carbene-promoted C(sp<sup>3</sup>)-H oxidative coupling of isochromans and triazoles was developed in up to 83% yield at room temperature in air. The radical-like triplet carbenes were used as efficient HAT acceptors, and the possible synergistic HAT enabled the unprecedented process with a high regioselectivity.

The Journal of Organic ChemistryVol. 90(12)
East China Normal University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Chongqing
Clean water and sanitation
Openalex Percentile: Top 11%
Catalytic C–H Functionalization Methods
2.81
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